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	<title><![CDATA[BOL: Related items]]></title>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36861/eagler-a-scaffolding-tool-for-long-reads</guid>
	<pubDate>Mon, 04 Jun 2018 05:26:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36861/eagler-a-scaffolding-tool-for-long-reads</link>
	<title><![CDATA[EAGLER: a scaffolding tool for long reads.]]></title>
	<description><![CDATA[<p>EAGLER is a scaffolding tool for long reads. The scaffolder takes as input a draft genome created by any NGS assembler and a set of long reads. The long reads are used to extend the contigs present in the NGS draft and possibly join overlapping contigs. EAGLER supports both PacBio and Oxford Nanopore reads.</p>
<p>The tool should be compatible with most UNIX flavors and has been successfully tested on the following operating systems:</p>
<ul>
<li>Mac OS X 10.11.1</li>
<li>Mac OS X 10.10.3</li>
<li>Ubuntu 14.04 LTS</li>
</ul>

https://bib.irb.hr/datoteka/844447.Diplomski_2015_Luka_terbi.pdf<p>Address of the bookmark: <a href="https://github.com/mculinovic/EAGLER" rel="nofollow">https://github.com/mculinovic/EAGLER</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37473/lsc-a-long-read-error-correction-tool</guid>
	<pubDate>Thu, 02 Aug 2018 07:39:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37473/lsc-a-long-read-error-correction-tool</link>
	<title><![CDATA[LSC :a long read error correction tool]]></title>
	<description><![CDATA[<h2>Getting Started</h2>
<p>These simple steps will help you integrate LSC into your transcriptomics analysis pipeline.</p>
<ul>
<li>Read the&nbsp;<a href="https://www.healthcare.uiowa.edu/labs/au/LSC/LSC_requirements.asp">LSC_requirements</a>&nbsp;for running LSC.</li>
<li><a href="https://www.healthcare.uiowa.edu/labs/au/LSC/LSC_download.asp">Download</a>&nbsp;and set-up the LSC package.</li>
<li>Follow the&nbsp;<a href="https://www.healthcare.uiowa.edu/labs/au/LSC/LSC_tutorial.asp">tutorial</a>&nbsp;to see how LSC works on some example data.</li>
<li>Read the&nbsp;<a href="https://www.healthcare.uiowa.edu/labs/au/LSC/LSC_manual.asp">manual</a>&nbsp;if anything is unclear.</li>
<li>You're ready, Happy LSCing!</li>
</ul>
<h2>Latest publication</h2>
<p><span>Kin Fai Au, Jason Underwood, Lawrence Lee and Wing Hung Wong&nbsp;</span><br><strong>Improving PacBio Long Read Accuracy by Short Read Alignment&nbsp;</strong><span>[</span><a href="http://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0046679">Manuscript</a><span>]&nbsp;</span><br><em>PLoS ONE</em><span>&nbsp;2012. 7(10): e46679. doi:10.1371/journal.pone.0046679</span></p><p>Address of the bookmark: <a href="https://www.healthcare.uiowa.edu/labs/au/LSC/" rel="nofollow">https://www.healthcare.uiowa.edu/labs/au/LSC/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37576/lrcstats-a-tool-for-evaluating-long-reads-correction-methods</guid>
	<pubDate>Wed, 22 Aug 2018 11:05:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37576/lrcstats-a-tool-for-evaluating-long-reads-correction-methods</link>
	<title><![CDATA[LRCstats: a tool for evaluating long reads correction methods]]></title>
	<description><![CDATA[<p><span>LRCstats is an open-source pipeline for benchmarking DNA long read correction algorithms for long reads outputted by third generation sequencing technology such as machines produced by Pacific Biosciences. The reads produced by third generation sequencing technology, as the name suggests, are longer in length than reads produced by next generation sequencing technologies, such as those produced by Illumina. However, long reads are plagued by high error rates, which can cause issues in downstream analysis. Long read correction algorithms reduce the error rate of long reads either through self-correcting methods or using accurate, short reads outputted by next generation sequencing technologies to correct long reads.</span></p><p>Address of the bookmark: <a href="https://github.com/cchauve/lrcstats" rel="nofollow">https://github.com/cchauve/lrcstats</a></p>]]></description>
	<dc:creator>Aaryan Lokwani</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37837/clipcrop-a-tool-for-detecting-structural-variations-with-single-base-resolution-using-soft-clipping-information</guid>
	<pubDate>Thu, 04 Oct 2018 16:39:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37837/clipcrop-a-tool-for-detecting-structural-variations-with-single-base-resolution-using-soft-clipping-information</link>
	<title><![CDATA[ClipCrop: a tool for detecting structural variations with single-base resolution using soft-clipping information]]></title>
	<description><![CDATA[<p>This is a tool for detecting structural variations using soft-clipping information From&nbsp;<a href="http://samtools.sourceforge.net/SAM1.pdf">SAM</a>&nbsp;files.</p>
<p>https://github.com/shinout/clipcrop</p><p>Address of the bookmark: <a href="https://github.com/shinout/clipcrop" rel="nofollow">https://github.com/shinout/clipcrop</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38561/hawkeye-an-interactive-visual-analytics-tool-for-genome-assemblies</guid>
	<pubDate>Tue, 01 Jan 2019 11:56:17 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38561/hawkeye-an-interactive-visual-analytics-tool-for-genome-assemblies</link>
	<title><![CDATA[Hawkeye: an interactive visual analytics tool for genome assemblies]]></title>
	<description><![CDATA[<p><span>Genome sequencing remains an inexact science, and genome sequences can contain significant errors if they are not carefully examined. Hawkeye is our new visual analytics tool for genome assemblies, designed to aid in identifying and correcting assembly errors. Users can analyze all levels of an assembly along with summary statistics and assembly metrics, and are guided by a ranking component towards likely mis-assemblies. Hawkeye is freely available and released as part of the open source AMOS project&nbsp;</span><span><a href="http://amos.sourceforge.net/hawkeye"><span>http://amos.sourceforge.net/hawkeye</span></a></span><span>.</span></p>
<p>https://genomebiology.biomedcentral.com/articles/10.1186/gb-2007-8-3-r34</p><p>Address of the bookmark: <a href="http://amos.sourceforge.net/wiki/index.php?title=Hawkeye" rel="nofollow">http://amos.sourceforge.net/wiki/index.php?title=Hawkeye</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39728/patterns-a-modeling-tool-dedicated-to-biological-network-modeling</guid>
	<pubDate>Fri, 26 Jul 2019 01:11:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39728/patterns-a-modeling-tool-dedicated-to-biological-network-modeling</link>
	<title><![CDATA[Patterns: a modeling tool dedicated to biological network modeling]]></title>
	<description><![CDATA[<p>It is designed to work with <strong>patterned data</strong>. Famous examples of problems related to patterned data are:</p>
<ul>
<li>recovering <strong>signals</strong> in networks after a <strong>stimulation</strong> (cascade network reverse engineering),</li>
<li>analysing <strong>periodic signals</strong>.</li>
</ul><p>Address of the bookmark: <a href="https://github.com/fbertran/Patterns" rel="nofollow">https://github.com/fbertran/Patterns</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41125/chromonomer-a-tool-set-for-repairing-and-enhancing-assembled-genomes-through-integration-of-genetic-maps-and-conserved-synteny</guid>
	<pubDate>Mon, 17 Feb 2020 05:38:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41125/chromonomer-a-tool-set-for-repairing-and-enhancing-assembled-genomes-through-integration-of-genetic-maps-and-conserved-synteny</link>
	<title><![CDATA[Chromonomer: a tool set for repairing and enhancing assembled genomes through integration of genetic maps and conserved synteny]]></title>
	<description><![CDATA[<p>Chromonomer is a program designed to integrate a genome assembly with a genetic map. Chromonomer tries very hard to identify and remove markers that are out of order in the genetic map, when considered against their local assembly order; and to identify scaffolds that have been incorrectly assembled according to the genetic map, and split those scaffolds.</p><p>Address of the bookmark: <a href="http://catchenlab.life.illinois.edu/chromonomer/" rel="nofollow">http://catchenlab.life.illinois.edu/chromonomer/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41916/truvari-structural-variant-comparison-tool-for-vcfs</guid>
	<pubDate>Tue, 30 Jun 2020 21:30:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41916/truvari-structural-variant-comparison-tool-for-vcfs</link>
	<title><![CDATA[truvari: Structural variant comparison tool for VCFs]]></title>
	<description><![CDATA[<p>Structural variant comparison tool for VCFs</p>
<p>Given benchmark and comparsion sets of SVs, calculate the recall, precision, and f-measure.</p>
<p><a href="https://github.com/spiralgenetics/www.spiralgenetics.com">Spiral Genetics</a></p>
<p><a href="https://docs.google.com/presentation/d/17mvC1XOpOm7khAbZwF3SgtG2Rl4M9Mro37yF2nN7GhE/edit">Motivation</a></p><p>Address of the bookmark: <a href="https://github.com/spiralgenetics/truvari" rel="nofollow">https://github.com/spiralgenetics/truvari</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42143/sibelia-a-comparative-genomics-tool</guid>
	<pubDate>Sat, 22 Aug 2020 02:49:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42143/sibelia-a-comparative-genomics-tool</link>
	<title><![CDATA[Sibelia: A comparative genomics tool]]></title>
	<description><![CDATA[<p><strong>Sibelia</strong>: A comparative genomics tool: It assists biologists in analysing the genomic variations that correlate with pathogens, or the genomic changes that help microorganisms adapt in different environments. Sibelia will also be helpful for the evolutionary and genome rearrangement studies for multiple strains of microorganisms.&nbsp;</p>
<p><strong>Sibelia</strong>&nbsp;is useful in finding: (1) shared regions, (2) regions that present in one group of genomes but not in others, (3) rearrangements that transform one genome to other genomes.</p>
<p>More at&nbsp;<a href="http://bioinf.spbau.ru/sibelia">http://bioinf.spbau.ru/sibelia</a></p>
<p>Sibelia docs&nbsp;<a href="http://gensoft.pasteur.fr/docs/Sibelia/3.0.7/SIBELIA.md">http://gensoft.pasteur.fr/docs/Sibelia/3.0.7/SIBELIA.md</a></p><p>Address of the bookmark: <a href="https://github.com/bioinf/Sibelia" rel="nofollow">https://github.com/bioinf/Sibelia</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43120/ventoy-an-open-source-tool-to-create-bootable-usb-drive</guid>
	<pubDate>Tue, 29 Jun 2021 10:16:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43120/ventoy-an-open-source-tool-to-create-bootable-usb-drive</link>
	<title><![CDATA[Ventoy: an open source tool to create bootable USB drive]]></title>
	<description><![CDATA[<p>Ventoy is an open source tool to create bootable USB drive for ISO/WIM/IMG/VHD(x)/EFI files. With ventoy, you don't need to format the disk over and over, you just need to copy the image files to the USB drive and boot it. You can copy many image files at a time and ventoy will give you a boot menu to select them. x86 Legacy BIOS, IA32 UEFI, x86_64 UEFI, ARM64 UEFI and MIPS64EL UEFI are supported in the same way. Both MBR and GPT partition style are supported in the same way. Most type of OS supported(Windows/WinPE/Linux/Unix/Vmware/Xen...) 700+ ISO files are tested.&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/ventoy/Ventoy" rel="nofollow">https://github.com/ventoy/Ventoy</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>

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